| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75480550-75481320 | Common:39; Rare:316; Clinvar (benign):2 | ||||
| chr13:78658360-78658630 | Rare:112 | ||||
| chr13:91348760-91349220 | Common:11; Rare:322 | ||||
| chr13:93228370-93228933 | Common:2; Rare:212 | ||||
| chr13:95122140-95122350 | Rare:40 | ||||
| chr13:95123700-95124246 | Common:4; Rare:150 | ||||
| chr13:95533871-95534006 | Common:1; Rare:32 | ||||
| chr13:97432910-97433320 | Common:5; Rare:117 | ||||
| chr13:98033630-98034279 | Common:2; Rare:201 | ||||
| chr13:98212980-98213530 | Common:6; Rare:214 | ||||
| chr13:98266291-98266691 | Common:11; Rare:98 | ||||
| chr13:98267060-98267438 | Common:5; Rare:128 | ||||
| chr13:98269360-98269769 | Rare:107 | ||||
| chr13:98301246-98301352 | Common:1; Rare:22 | ||||
| chr13:99496613-99497000 | Common:3; Rare:156 |